HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Indopan, (+)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (S)-2-amino-1-(1H-indol-3-yl)-propan-1-one | HCID 12993396 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Indopan, (+)- | HCID 854157 | — |
Reaction Steps
A solution of (S)-2-amino-1-(1H-indol-3-yl)-propan-1-one (0.47 g, 2.5 mmol, 1.0 eq.) in acetonitrile and isopropanol is treated portionwise with NaBH4 (285 mg, 7.49 mmol, 3.0 equiv.), heated at reflux temperature for 24 h, stirred at room temperature under N2 for 36 h, quenched with methanol, concentrated and partitioned between water and EtOAc. The EtOAc phase is dried over MgSO4 and concentrated in vacuo to afford the title product as a brown oil, identified by HPLC and mass spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06770642B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-00f191d7c9be496b9dba3aa8cf8d939c |
| Source note | uspto-grants-2004_08 |